体内
化学
细胞生物学
纳米技术
材料科学
生物
生物技术
作者
Pritha Agarwalla,Edikan A. Ogunnaike,Sarah Ahn,Kristen Froehlich,Anton Jansson,Frances S. Ligler,Gianpietro Dotti,Yevgeny Brudno
标识
DOI:10.1038/s41587-022-01245-x
摘要
Despite their clinical success, chimeric antigen receptor (CAR)-T cell therapies for B cell malignancies are limited by lengthy, costly and labor-intensive ex vivo manufacturing procedures that might lead to cell products with heterogeneous composition. Here we describe an implantable Multifunctional Alginate Scaffold for T Cell Engineering and Release (MASTER) that streamlines in vivo CAR-T cell manufacturing and reduces processing time to a single day. When seeded with human peripheral blood mononuclear cells and CD19-encoding retroviral particles, MASTER provides the appropriate interface for viral vector-mediated gene transfer and, after subcutaneous implantation, mediates the release of functional CAR-T cells in mice. We further demonstrate that in vivo-generated CAR-T cells enter the bloodstream and control distal tumor growth in a mouse xenograft model of lymphoma, showing greater persistence than conventional CAR-T cells. MASTER promises to transform CAR-T cell therapy by fast-tracking manufacture and potentially reducing the complexity and resources needed for provision of this type of therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI